Distinctive Sources Govern Organic Aerosol Fractions with Different Degrees of Oxygenation in the Urban Atmosphere

气溶胶 化学 背景(考古学) 生物质燃烧 环境化学 有机质 大气(单位) 分馏 质谱 质谱法 微粒 气象学 有机化学 色谱法 生物 古生物学 物理
作者
Ruichen Zhou,Qingcai Chen,Jing Chen,Lujie Ren,Yange Deng,Petr Vodička,Dhananjay K. Deshmukh,Kimitaka Kawamura,Pingqing Fu,Michihiro Mochida
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:55 (8): 4494-4503 被引量:10
标识
DOI:10.1021/acs.est.0c08604
摘要

Understanding how the sources of an atmospheric organic aerosol (OA) govern its burden is crucial for assessing its impact on the environment and adopting proper control strategies. In this study, the sources of OA over Beijing were assessed year-around based on the combination of two separation approaches for OA, one from chemical fractionation into the high-polarity fraction of water-soluble organic matter (HP-WSOM), humic-like substances (HULIS), and water-insoluble organic matter (WISOM), and the other from statistical grouping using positive matrix factorization (PMF) of high-resolution aerosol mass spectra. Among the three OA fractions, HP-WSOM has the highest O/C ratio (1.36), followed by HULIS (0.56) and WISOM (0.17). The major sources of different OA fractions were distinct: HP-WSOM was dominated by more oxidized oxygenated OA (96%); HULIS by cooking-like OA (40%), less oxidized oxygenated OA (27%), and biomass burning OA (21%); and WISOM by fossil fuel OA (77%). In addition, our results provide evidence that mass spectral-based PMF factors are associated with specific substructures in molecules. These structures are further discussed in the context of the FT-IR results. This study presents an overall relationship of OA groups monitored by chemical and statistical approaches for the first time, providing insights for future source apportionment studies.

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